Streamline variant analysis

Discover how Alamut™ Visual Plus can make advanced variant analysis scalable and accessible in your lab.

Gain time with an intuitive interface and strong customer support

Improve productivity with efficient and user-friendly data-to-report workflows

Enhance variant analysis by accessing 50+ curated sources of information in a single place

Scale your projects with software that remains accessible to all types of users, from beginners to skilled bioinformaticians

Get started with a free trial

Discover how Alamut™ Visual Plus will support
your analysis of disease-associated variants

Supports a large number of file types

Allows you to import and visualize BAM, VCF, BED, and Sanger files

Integrates highly sensitive predictors

Simplifies access to splicing and missense predictors such as MaxEntScan, NNSPLICE, SIFT, and PolyPhen-2

Combines multiple curated databases

Integrates information from databases such as ClinVar, dbSNP, BRIDGES, CADD, PubMed®, and MasterMind®

Simplifies genomic data visualization

Empowers you to visualize flanking and overlapping regions, and explore several genes at once in the nuclear and mitochondrial genomes

Keeps your
data safe

Secures your most sensitive information

Grows with your needs

New features are regularly added to improve your experience and support your needs